Evidence map›Paper›PMID 34685399›Full record

ArticleLife (Basel, Switzerland)2021

NMUR1 in the NMU-Mediated Regulation of Bone Remodeling.

Yu-Tin Hsiao, Kelli J Manikowski, Samantha Snyder, Nicole Griffin, Ashley L Orr, Elizabeth Q Hulsey, Gabriella Born-Evers, Tara Zukosky, Maria E Squire, Julia M Hum and 3 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 54% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Thrombopoietic agents enhance bone healing in mice, rats, and pigs.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Yu-Tin HsiaoDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Kelli J ManikowskiDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Samantha SnyderDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Nicole GriffinDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Ashley L OrrDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Elizabeth Q HulseyDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Gabriella Born-EversDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Tara ZukoskyDepartment of Biology, The University of Scranton, Scranton, PA 18503, USA.
Maria E SquireDepartment of Biology, The University of Scranton, Scranton, PA 18503, USA.
Julia M HumDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.
Corinne E MetzgerDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Matthew R AllenDepartment of Anatomy, Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Jonathan W LoweryDivision of Biomedical Science, Marian University College of Osteopathic Medicine, Indianapolis, IN 46022, USA.ORCID 0000-0002-9942-2945
Marian University - Indiana · USIndiana University School of MedicineUniversity of Scranton · US

Funding

Marian University N/A
6 · The paper itself

Abstract

Neuromedin-U (NMU) is an evolutionarily conserved peptide that regulates varying physiologic effects including blood pressure, stress and allergic responses, metabolic and feeding behavior, pain perception, and neuroendocrine functions. Recently, several lines of investigation implicate NMU in regulating bone remodeling. For instance, global loss of NMU expression in male and female mice leads to high bone mass due to elevated bone formation rate with no alteration in bone resorption rate or observable defect in skeletal patterning. Additionally, NMU treatment regulates the activity of osteoblasts in vitro. The downstream pathway utilized by NMU to carry out these effects is unknown as NMU signals via two G-protein-coupled receptors (GPCRs), NMU receptor 1 (NMUR1), and NMU receptor 2 (NMUR2), and both are expressed in the postnatal skeleton. Here, we sought to address this open question and build a better understanding of the downstream pathway utilized by NMU. Our approach involved the knockdown of

Indexed as

boneNeuromedin-UNMUNMUR1NMUR2osteoblastosteoporosis

Identifiers

PMID34685399
PMCPMC8538501
OpenAlexW3204488363

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.